Satanay Z. Hubrack

Doha, DA, Qatar

Last Updated: 09/26/2026

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Found 27 publications

Genomic diagnosis and multisystem phenotyping in pediatric congenital analbuminemia: clinical, coagulation, and immune signatures.

Genomic diagnosis and multisystem phenotyping in pediatric congenital analbuminemia: clinical, coagulation, and immune signatures.

Journal: Frontiers in pediatrics

Published: February 13, 2026

Autosomal recessive A20 zinc finger 7 mutation is associated with early-onset lupus-like disease.

Autosomal recessive A20 zinc finger 7 mutation is associated with early-onset lupus-like disease.

Journal: Inflammation research : official journal of the European Histamine Research Society ... [et al.]

Published: November 19, 2025

A homozygous CTLA-4 variant causes CTLA-4 deficiency with severe immune dysregulation.

A homozygous CTLA-4 variant causes CTLA-4 deficiency with severe immune dysregulation.

Journal: Journal of human immunity

Published: October 20, 2025

Abatacept restores dysregulated transcriptomic and proteomic profile in disorders of CTLA-4 insufficiency.

Abatacept restores dysregulated transcriptomic and proteomic profile in disorders of CTLA-4 insufficiency.

Journal: The Journal of allergy and clinical immunology

Published: June 04, 2025

The Complex Etiology of Epilepsy: Genetic Analysis and HLA Association in Patients in the Middle East.

The Complex Etiology of Epilepsy: Genetic Analysis and HLA Association in Patients in the Middle East.

Journal: International journal of molecular sciences

Published: April 15, 2025

Biallelic Loss-of-Function Variant in MINPP1 Causes Pontocerebellar Hypoplasia with Characteristic Severe Neurodevelopmental Disorder.

Biallelic Loss-of-Function Variant in MINPP1 Causes Pontocerebellar Hypoplasia with Characteristic Severe Neurodevelopmental Disorder.

Journal: International journal of molecular sciences

Published: March 28, 2025

Dual variants of uncertain significance in a case of hyper-IgM syndrome: implications for diagnosis and management.

Dual variants of uncertain significance in a case of hyper-IgM syndrome: implications for diagnosis and management.

Journal: Frontiers in immunology

Published: March 16, 2025

MUC2 expression modulates immune infiltration in colorectal cancer.

MUC2 expression modulates immune infiltration in colorectal cancer.

Journal: Frontiers in immunology

Published: September 23, 2024

Systematic comparison of quantity and quality of RNA recovered with commercial FFPE tissue extraction kits.

Systematic comparison of quantity and quality of RNA recovered with commercial FFPE tissue extraction kits.

Journal: Journal of translational medicine

Published: September 03, 2024

Loss of the TRPM4 channel in humans causes immune dysregulation with defective monocyte migration.

Loss of the TRPM4 channel in humans causes immune dysregulation with defective monocyte migration.

Journal: The Journal of allergy and clinical immunology

Published: June 07, 2023

Chronic reduction of store operated Ca2+ entry is viable therapeutically but is associated with cardiovascular complications.

Chronic reduction of store operated Ca2+ entry is viable therapeutically but is associated with cardiovascular complications.

Journal: The Journal of physiology

Published: September 05, 2022

Biallelic TLR4 deficiency in humans.

Biallelic TLR4 deficiency in humans.

Journal: The Journal of allergy and clinical immunology

Published: June 16, 2022

Showing 1-12 of 27

Last Updated: 09/26/2026